Affiliation:
1. Department of Biology, Emory University, Atlanta, Georgia 30322
Abstract
ABSTRACT
We have examined the expression of the
rpsO-pnp
operon in an RNase III (
rnc
) mutant of
Streptomyces coelicolor
. Western blotting demonstrated that polynucleotide phosphorylase (PNPase) levels increased in the
rnc
mutant, JSE1880, compared with the parental strain, M145, and this observation was confirmed by polymerization assays. It was observed that
rpsO-pnp
mRNA levels increased in the
rnc
mutant by 1.6- to 4-fold compared with M145. This increase was observed in exponential, transition, and stationary phases, and the levels of the readthrough transcript, initiated upstream of
rpsO
in the
rpsO-pnp
operon; the
pnp
transcript, initiated in the
rpsO-pnp
intergenic region; and the
rpsO
transcript all increased. The increased levels of these transcripts in JSE1880 reflected increased chemical half-lives for each of the three. We demonstrated further that overexpression of the
rpsO
-
pnp
operon led to significantly higher levels of PNPase activity in JSE1880 compared to M145, reflecting the likelihood that PNPase expression is autoregulated in an RNase III-dependent manner in
S. coelicolor
. To explore further the increase in the level of the
pnp
transcript initiated in the intergenic region in JSE1880, we utilized that transcript as a substrate in assays employing purified
S. coelicolor
RNase III. These assays revealed the presence of hitherto-undiscovered sites of RNase III cleavage of the
pnp
transcript. The position of those sites was determined by primer extension, and they were shown to be situated in the loops of a stem-loop structure.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
15 articles.
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